Literature DB >> 5489000

Non-condensation of one segment of a chromosome No. 2 in a male with an otherwise normal karyotype (and severe hypospadias).

E M Bühler, U Luchsinger, U K Bühler, K Méhes, G R Stalder.   

Abstract

Entities:  

Mesh：

Year:  1970        PMID： 5489000     DOI： 10.1007/bf00696019

Source DB:  PubMed          Journal:  Humangenetik        ISSN： 0018-7348


× No keyword cloud information.
  27 in total

1.  The sites and relative frequencies of secondary constrictions in human somatic chromosomes.

Authors:  M A FERGUSON-SMITH; M E FERGUSON-SMITH; P M ELLIS; M DICKSON
Journal:  Cytogenetics       Date:  1962

2.  Enlarged chromosome No. 1 in a patient with primary amenorrhoea.

Authors:  J Philip; O Frydenberg; V Sele
Journal:  Cytogenetics       Date:  1965

3.  [Selective endoreduplication of the long arm of the 2 chromosome in a woman and her daughter].

Authors:  J Lejeune; B Dutrillaux; J Lafourcade; R Berger; D Abonyi; M O Rethoré
Journal:  C R Acad Hebd Seances Acad Sci D       Date:  1968-01-03

4.  [Two observations of identical breakages in the same group C chromosome].

Authors:  I Emerit; J De Grouchy; P Vernant
Journal:  Ann Genet       Date:  1968-03

5.  Asynchrony of DNA replication and mitotic spiralization along heterochromatic portions of Chinese hamster chromosomes.

Authors:  A F Zakharov; N A Egolina
Journal:  Chromosoma       Date:  1968       Impact factor: 4.316

6.  Chromosomal changes of similar nature in seven established cell lines derived from the peripheral blood of patients with leukemia.

Authors:  H zur Hausen
Journal:  J Natl Cancer Inst       Date:  1967-05       Impact factor: 13.506

Review 7.  The cri-du-chat syndrome with an apparently normal karyotype.

Authors:  D D McGavin; J S Cant; M A Ferguson-Smith; P M Ellis
Journal:  Lancet       Date:  1967-08-12       Impact factor: 79.321

8.  Chromosome abnormality and hypocalcemia in congenital erythroid hypoplasia. (Blackfan-Diamond syndrome).

Authors:  A P Tartaglia; S Propp; A P Amarose; R P Propp; C A Hall
Journal:  Am J Med       Date:  1966-12       Impact factor: 4.965

9.  Familial congenital heart disease. II. Chromosomal studies.

Authors:  J German; K H Ehlers; M A Engle
Journal:  Circulation       Date:  1966-09       Impact factor: 29.690

10.  3H labeling patterns of permanent cell line chromosomes showing pulverization or accentuated secondary constrictions.

Authors:  C P Miles; F O'Neill
Journal:  J Cell Biol       Date:  1969-02       Impact factor: 10.539
View more
  9 in total

1.  Heritable fragile sites on human chromosomes I. Factors affecting expression in lymphocyte culture.

Authors:  G R Sutherland
Journal:  Am J Hum Genet       Date:  1979-03       Impact factor: 11.025

2.  Studies on three rare fragile sites. 2q13, 12q13, and 17p12 segregating in one family.

Authors:  D R Romain; L M Columbano-Green; R H Smythe; R G Parfitt; O B Gebbie; C J Chapman
Journal:  Hum Genet       Date:  1986-06       Impact factor: 4.132

3.  The constitutional fragility of chromosome 12 in a case of 46,XX,var(12)(gh',RHG,CAG,CBG).

Authors:  E Donti; G Venti; V Bocchini; G Rosi; R Armellini; N Trabalza
Journal:  Hum Genet       Date:  1979-04-17       Impact factor: 4.132

4.  Heritable fragile sites on human chromosomes II. Distribution, phenotypic effects, and cytogenetics.

Authors:  G R Sutherland
Journal:  Am J Hum Genet       Date:  1979-03       Impact factor: 11.025

5.  Structural aberration in chromosome no.2.

Authors:  J Nielsen
Journal:  Humangenetik       Date:  1973-09-20

6.  Variations in karyotypes of normal premature babies, new-born babies and infants.

Authors:  H Müller
Journal:  Humangenetik       Date:  1971

7.  Constitutional chromosomal breakage.

Authors:  F Giraud; S Ayme; J F Mattei; M G Mattei
Journal:  Hum Genet       Date:  1976-10-28       Impact factor: 4.132

Review 8.  Familial fragile secondary constriction on chromosome 2 (2q11) with unusual features and psychomotor retardation.

Authors:  D S Murthy; A S Teebi; T S Sundareshan; S A al-Awadi
Journal:  Indian J Pediatr       Date:  1990 Mar-Apr       Impact factor: 1.967

9.  Expression in fibroblast culture of the satellited-X chromosome associated with familial sex-linked mental retardation.

Authors:  P B Jacky; F J Dill
Journal:  Hum Genet       Date:  1980-02       Impact factor: 4.132
  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.